US6083308A - Anti-corrosive pigment and compositions formulated with such pigments - Google Patents

Anti-corrosive pigment and compositions formulated with such pigments Download PDF

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US6083308A
US6083308A US09/029,478 US2947898A US6083308A US 6083308 A US6083308 A US 6083308A US 2947898 A US2947898 A US 2947898A US 6083308 A US6083308 A US 6083308A
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acid
polyvalent metal
organophosphonate
corrosive
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Tim Fletcher
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Grace GmbH
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    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK  ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
    • C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
    • C09C1/0081—Composite particulate pigments or fillers, i.e. containing at least two solid phases, except those consisting of coated particles of one compound
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L43/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing boron, silicon, phosphorus, selenium, tellurium or a metal; Compositions of derivatives of such polymers
    • C08L43/02—Homopolymers or copolymers of monomers containing phosphorus
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B57/00—Other synthetic dyes of known constitution
    • C09B57/10—Metal complexes of organic compounds not being dyes in uncomplexed form
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D143/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing boron, silicon, phosphorus, selenium, tellurium, or a metal; Coating compositions based on derivatives of such polymers
    • C09D143/02—Homopolymers or copolymers of monomers containing phosphorus
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/08—Anti-corrosive paints
    • C09D5/082—Anti-corrosive paints characterised by the anti-corrosive pigment
    • C09D5/086—Organic or non-macromolecular compounds
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/02—Non-macromolecular additives
    • C09J11/06—Non-macromolecular additives organic
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00—Particle morphology
    • C01P2004/80—Particles consisting of a mixture of two or more inorganic phases

Definitions

  • Examples of existing commercial lower or non-toxic alternative pigments are metal salts of phosphates, phosphosilicates, borosiicates, borates, metaborates, molybdates, polyphosphates, triphosphates and phosphites using typically calcium, strontium, barium, zinc and aluminium as the metallic cations.
  • Ion-exchanged silicas such as calcium-exchanged silica have also been introduced.
  • Zinc phosphate is currently by far the most widely used low or non-toxic anti-corrosive pigment.
  • the non-toxic alternative pigments are sometimes used in combinations of two or more pigments in an effort to improve performance levels. This approach has met with varying degrees of success.
  • the use of combinations of pigments naturally adds to the complexities involved in coating development and manufacture.
  • Organophosphonic acids and their water-soluble salts are known in the field of water treatment chemicals where they are used to help inhibit is scale formation and metal corrosion. These compounds are added to water systems such as cooling water and boiler water at very low concentrations, typically in the ppm range.
  • the formulation of an effective water treatment chemical is very complex, but to exert adequate corrosion inhibition, such organophosphonic compounds are normally used in conjunction with ppm levels of polyvalent metal cations such as calcium and zinc.
  • anti-corrosion pigments suitable for incorporation into polymeric and protective materials such as coatings, adhesives, sealants and organic pretreatments
  • the anti-corrosive pigments of the invention provide performance superior to conventional lead and chromate free pigments and match the performance of the traditional pigments. Further, the anti-corrosion pigments of the invention achieve high anti-corrosive performance levels without the necessity to combine two or more different types of anti-corrosive pigment. Further, the anti-corrosion pigments of the invention achieve useful levels of anti-corrosive performance without the need for addition of heavy metals and/or zinc.
  • the invention encompasses anti-corrosion pigments which contain polyvalent metal salts of organophosphonic compound(s) in the basic state.
  • the organophosphonic compound(s) may contain one or more phosphonic groups per molecule.
  • Preferred organophosphonic compounds are phosphonocarboxylic acids such as 2-hydroxy-2-phosphonoacetic acid, or 2-phosphono-1,2,4-tricarboxylic acid and phosphonates such as nitrilotris(methylenephosphonic) acid, 1-hydroxyethane(1,1-iphosphonic acid) and phosphonated derivatives of acrylic acid and maleic acid. If desired, mixtures of different organophosphonic compounds and/or different polyvalent metals may be used.
  • the invention encompasses pigments containing neutral to basic polyvalent metal salts of organophosphonic compound components combined with a co-acid component.
  • the combination of these components is preferably done during pigment preparation by partial replacement of the organophosphonic compound with the co-acid, whereby at least a portion of the co-acid is reacted with polyvalent metal cations.
  • the co-acid is preferably polyvalent and may be solid or liquid co-acids like silicas, sheet silicates, crystalline aluminosilicates such as zeolites, other aluminosilicates and their combinations, phosphoric acid, polyphosphoric acid, boric acid or carboxylic acid derivatives such as maleic acid, polymaleic acid, polyacrylic acid and its derivatives or hydroxyacids like citric acid.
  • the invention further encompasses anti-corrosive coating compositions containing the pigments of the invention.
  • the coating compositions may be non-aqueous solvent-borne or water-borne anti-corrosive coatings.
  • the invention further encompasses methods for making the pigments and pigment-containing compositions of the invention.
  • the pigments of the invention are preferably produced in an aqueous environment by reaction of the appropriate organophosphonic compounds with the appropriate polyvalent metal cations.
  • the polyvalent metal cations may be introduced in various forms as oxides, hydroxides, carbonates, chlorides, nitrates or suiphates.
  • the reaction may be controlled by control of pH. Unwanted counter-ions may be removed by washing and/or thermal decomposition.
  • the pigments may then be further prepared by oven drying and milling, by wet-milling and spray drying or by other techniques to obtain the desired pigment particles.
  • Basic salts may be prepared using an excess of a sparingly soluble polyvalent metal oxide or hydroxide.
  • the polyvalent metal salts of organophosphonic compounds can be prepared as basic salts by addition of an excess of polyvalent metal cations during preparation to produce effective anti-corrosive pigments which enable the formation of anti-corrosive coatings displaying a very high level of corrosion protection. It has further been discovered that neutral or basic polyvalent metal salts of organophosphonic compounds may be used in combination with a co-acid to produce effective anti-corrosive pigments which enable the formation of anti-corrosive coatings displaying a very high level of corrosion protection. These anti-corrosive pigments provide the possibility of obtaining a high level of corrosion protection while avoiding the use of heavy metals.
  • the organophosphonic compounds useful in the invention may contain one or more phosphonic groups.
  • the initial organophosphonic compounds, reacted to form the pigments of the invention, may be in acid form, monovalent cation (e.g., alkali metal or ammonium) salt form, or in any other form suitable for use in forming the desired polyvalent metal cation salts.
  • the organophosphonic compounds may be used individually or in combination.
  • organophosphonic compounds containing one phosphonic (acid) group per molecule are phosphonocarboxylic acids such as 2-hydroxy-2-phosphonoacetic acid, 2-phosphonobutane-1,2,4-triacetic acid and phosphonated oligomers of maleic acid, acrylic acid ormaleic acid and acrylic acid cooligomers.
  • suitable organophosphonic compounds containing at least two phosphonic acid groups per molecule include diphosphonic acids such as alkylmethane-1-hydroxy-1,1-diphosphonic acids where the alkyl group may be substituted or unsubstituted having from 1-12 carbon atoms (e.g., methane-1-hydroxy-1,1-diphosphonic acid, or propane-1-hydroxy-1,1-diphosphonic acid).
  • diphosphonic acids such as alkylmethane-1-hydroxy-1,1-diphosphonic acids where the alkyl group may be substituted or unsubstituted having from 1-12 carbon atoms (e.g., methane-1-hydroxy-1,1-diphosphonic acid, or propane-1-hydroxy-1,1-diphosphonic acid).
  • Amino compounds containing two or more N-alkylene phosphonic acid groups may also be used to prepare poiyvalent metal salts according to the invention.
  • Examples of such amino compounds are alkylamino-di(alkylene phosphonic acids) where the alkyl group can be substituted or unsubstituted and have from 1 to 12 carbon atoms such as propyl, isopropyl, butyl, hexyl or 2-hydroxyethyl and the alkylene group may have from 1 to 5 carbon atoms; also amino-tri(alkylene phosphonic acids) such as nitrilo-tris-(methylene phosphonic acid) and nitrilo-tris-(propylene phosphonic acid).
  • alkylene diamine-tetra-(alkylene phosphonic acids) such as ethylene diamine-tetra-(methylene phosphonic acid
  • dialkylene triamine-penta-(alkylene phosphonic acids) such as diethylene triamine-penta-(methylene phosphonic acids), and so on.
  • phosphonic compounds most preferred are 2-hydroxy-2-phosphonoacetic acid, nitrilo-tris-(methylene phosphonic acid), 2-phosphonobutane-1,2,4-triacetic acid, 1-Hydroxyethane-1,1-diphosphonic acid, phosphonosuccinic acid and phosphonated oligomers of maleic acid, acrylic acid ormaleic acid and acrylic acid co-ligomers.
  • suitable polyvalent metal cations for use in the invention are cations of magnesium, calcium, strontium, barium, iron, cobalt. nickel, zinc, aluminium, titanium and zirconium.
  • Preferred cations are magnesium, calcium, zinc and aluminium.
  • the polyvalent metal cations may be used individually or as a mixture of two or more.
  • Preferred polyvalent metal combinations are calcium/zinc salts or calcium/magnesium salts.
  • the polyvalent metal cations may be used (i.e., reacted with the organophosphonic compound) in the form of oxides, hydroxides, carbonates, chlorides, sulphates, nitrates, oxalates or other compounds or mixtures of is such compounds.
  • the polyvalent metal cations are in the form of metal oxides or hydroxides.
  • basic salts preferably sparingly soluble (solubility at 20° C. of less than 0.1 g/l) polyvalent metal oxides or hydroxides are used in excess.
  • suitable sparingly soluble metal oxides are zinc oxide, magnesium oxide, aluminium oxide, strontium oxide, barium oxide, cobalt oxide and nickel oxide. Particularly preferred are zinc oxide, magnesium oxide or magnesium hydroxide and alumina.
  • certain pigments of the invention may contain a combination of neutral or basic polyvalent metal salts of organophosphonic compounds with a co-acid.
  • the available acid sites of the co-acid are themselves preferably partially or completely reacted with polyvalent metal cations.
  • Suitable co-acids for use according to the invention can be divided into two classes: those which are water-soluble and those which can be considered essentially water-insoluble solids with replaceable surface hydrogen atoms such as silicas or silica aluminas.
  • suitable water-soluble co-acids include phosphoric acid or boric acid.
  • Compounds containing carboxylic acid groups which are water-soluble under the pigment preparation conditions may also be used; examples of such compounds include polycarboxylic acids such as maelic acid, succinic acid, azelaic acid, polymaleic acid and its derivatives, polyacrylic acid and its derivatives, and hydroxyacids such as tartaric acid and citric acid. In appropriate cases, adequate water solubility is achieved by use of the sodium or ammonium neutralised salts of the carboxylic acid-containing compounds.
  • essentially water-insoluble solid co-acids include silica, titania, zirconia, ferric oxide, sheet silicates, crystalline aluminosilicates such as zeolites, other aluminosilicates and their combinations. These solid co-acids may be used in there various colloidal and powder forms. Particularly preferred solid co-acids are silicas and silica aluminas, especially amorphous silicas or silica aluminas. If desired, the solid co-acid particles may be porous.
  • a neutral salt would correspond to a 1.5:1 molar ratio of zinc cation to organophosphonic compound (or a 1:1 equivalents ratio).
  • the equivalents ratio of polyvalent metal cations to acid groups preferably lies in the range of about 1.25:1 to 6:1, more preferably in the range of about 1.5:1 to 5:1.
  • the equivalents ratio of polyvalent metal cations to acid groups preferably lies in the range of about 1:1 to 6:1, more preferably in the range of about 1.25:1 to 5:1.
  • 1 mole of the acid may be reacted with from 1.5 to 9 moles of zinc oxide.
  • 1 mole of 2-phosphonobutane-1,2,4-triacetic acid may be reacted with from 2.5 to 15 moles of zinc oxide.
  • One mole of nitrilo-tris-(methylene phosphonic acid) may be reacted with from 3 to 18 moles of zinc oxide.
  • 1 mole of 2-hydroxy-2-phosphonoacetic acid may be reacted with up to 1.5 moles of calcium hydroxide and up to 12 moles (less the moles of calcium hydroxide used) of zinc oxide.
  • the neutral to basic polyvalent organophosphonates of the invention may be used in combination with co-acid(s). It should be understood that this replacement of part of the organophosphonic acid with a co-acid results in a chemical or physical combination of the organophosphonate and the co-acid (or its polyvalent metal salts) in the same pigment particle.
  • the organophosphonic compounds may be replaced with up to 95% (on an acid group basis) of water-soluble co-acids, more preferably about 5 to 75% on an acid group basis.
  • replacement of the organophosphonic compound can be made on the above-mentioned acid group basis where the amount of available acid groups in the solid co-acid is calculated based on the quantity of surface acid sites and available surface area.
  • the amount of solid acid used may simply be varied on a weight basis such that the pigment particles contain up to 95 wt. % of solid co-acid (Bronsted acid form, dry basis) based on the total weight of organophosphonic compound (Bronsted acid form, dry basis) and solid co-acid (Bronsted acid form, dry basis), more preferably 5 to 75 wt. %, most preferably about 25 to 60 wt. %.
  • the "Bronsted acid form” is meant to indicate that the available acid sites are occupied by H + ions. Within the ranges of co-acid, the most desired amount of replacement may be determined by actual corrosion protection tests and/or materials cost considerations.
  • the pigments of the invention are preferably prepared by processes involving the reaction of organophosphonic acid (or monovalent cation salt thereof, collectively referred to as "organophosphonic acid” below to simplify the discussion) with a source of polyvalent metal cations (typically a polyvalent metal compound).
  • organophosphonic acid or monovalent cation salt thereof, collectively referred to as "organophosphonic acid” below to simplify the discussion
  • a source of polyvalent metal cations typically a polyvalent metal compound.
  • the organophosphonic acid(s) is added to the polyvalent metal compound(s) in an aqueous medium.
  • the organophosphonic acids and the polyvalent metal cations in the resulting mixture undergo a reaction.
  • the reaction is allowed to occur to substantial completion as indicated by a stabilising of the pH.
  • the reaction mixture may be heated to accelerate the rate of reaction and/or to ensure completion of the reaction.
  • reaction mixture may be heated to temperatures of up to 95° C. (e.g. 40-95° C.) for periods up to 24 hours.
  • Mixing and uniformity of the reaction mixture can be achieved by a variety of conventional means such as simple stirring and high shear mixing or a combination of such techniques.
  • the various reactions useful in producing anti-corrosion pigments according to the invention may be conducted batchwise or continuously.
  • the source of poiyvalent metal cations is preferably a water-soluble salt such as a sulphate, chloride or nitrate.
  • the reaction mixture pH may be adjusted to an appropriate level (e.g., 6 to 9) by addition of a base such as sodium hydroxide or ammonium hydroxide to facilitate precipitation of the desired polyvalent metal organophosphonates.
  • a basic polyvalent metal organophosphonate salt i.e. greater than 1:1 polyvalent metal:acid group equivalents ratio
  • at least a portion of the source of polyvalent metal cations is in the form of a sparingly soluble compound (typically an oxide or hydroxide) which is added to the reaction mixture prior, during or after the addition of organophosphonic acid, but preferably before any thermal treatment, to create the requisite excess (above the 1:1 equivalents ratio) of polyvalent metal cation.
  • a sparingly soluble compound typically an oxide or hydroxide
  • Solid co-acids can be added at any stage prior to heating of the reaction mixture.
  • the solid co-acid is added to the aqueous medium before the addition of the organophosphonic acid such that the source of polyvalent metal cations and the co-acid come into contact before addition of the organophosphonic acid.
  • Water-soluble co-acids are preferably added at the same time as the organophosphonic acid.
  • the actual point of addition of the water-soluble co-acid especially the polycarboxylic co-acids mentioned above
  • the addition of any pH sensitive co-acid is preferably done at a pH which avoids loss of the benefits associated with addition of the co-acid.
  • the resulting pigments are preferably washed to remove any undesired ions.
  • the pigments may then be processed by conventional techniques to obtain particles of the desired size and physical integrity. For example, the pigments may be wet-milled followed by spray drying or may be oven-dried followed by milling to the desired particle size.
  • the pigments may be calcined in appropriate cases (e.g., to decompose undesired counter-ions, etc.).
  • Coating compositions containing the anticorrosion pigments of the invention can be prepared using virtually any water-based, non-aqueous solvent-based or solvent-free vehicle or resin known in the coatings industry.
  • the coating compositions may contain other typical ingredients appropriate for the resin system and intended application.
  • resin systems are those based on oleoresins, alkyd resins and modified alkyd resins, epoxy resins and epoxy esters, chlorinated rubbers, vinyl resins, butyral resins, polyurethanes, polyesters, acrylic polymers, amino resins, polyamines, polyamides, organic and inorganic silicates, hydrocarbon resins and styreneacrylic resins.
  • the anti-corrosive pigments of the invention may also be used in other polymer-containing materials such as adhesives, sealants, and elastomers.
  • HPA hydroxyphosphonoacetic acid (sold commercially as BELCOR 575).
  • ATMP nitrilotris-(methylenephosphonic) acid (sold commercially as DEQUEST 2000 or BRI-PHOS 301-50A).
  • a suspension of 44.20 g of calcium hydroxide (0.6 moles) in 362.00 g of demineralised water was prepared. Under constant stirring, 124.24 g of a 50% solution of HPA (0.4 moles) was added over a period of about 35 minutes at a rate oft 3 ml/minute. During the addition, the temperature reached about 40-50° C.
  • the reaction mixture was heated to 90° C. and aged for 1 hour. The mixture was then allowed to stand under slow stirring at room temperature for a further 16 hours. The resulting brown precipitate was washed by centrifugation, oven dried at 120° C. for 16 hours and milled.
  • the product yield was 92 g.
  • a suspension of 48.60 g of zinc oxide (0.6 moles) in 362.00 g of demineralised water was prepared. Under constant stirring, 124.80 g of a 50% solution of HPA (0.4 moles) was added over a period of about 35 minutes at a rate of 3 ml/minute. During the addition, the temperature reached about 40-50° C. The reaction mixture was heated to 90° C. and aged for 1 hour. The mixture was then allowed to stand at room temperature for a further 16 hours. The resulting slightly brown precipitate was washed by centrifugation, oven dried at 120° C. for 16 hours and milled. The product yield was 102 g.
  • a suspension of 48.60 g of zinc oxide (0.6 moles) in 362.00 g of demineralised water was prepared. Under constant stirring, 124.80 g of a 50% solution of HPA (0.4 moles) was added over a period of about 35 minutes at a rate of 3 ml/minute. During the addition, the temperature reached about 40-50° C. After the pH had stabilised, a further 145.80 g of zinc oxide (1.80 moles) was stirred in. The reaction mixture was heated to 90° C. and aged for 1 hour. The mixture was then allowed to stand at room temperature for a further 16 hours. The resulting brown precipitate was washed by centrifugation, oven dried at 120° C. for 16 hours and milled. The product yield was 233 g.
  • a suspension of 44.20 g of calcium hydroxide (0.6 moles) in 362.00 g of demineralised water was prepared. Under constant stirring, 124.80 g of a 50% solution of HPA (0.4 moles) was added over a period of about 35 minutes at a rate of 3 ml/minute. During the addition, the temperature reached about 40-50° C. After the pH had stabilised, a further 48.40 g of zinc oxide (0.60 moles) was stirred in. The reaction mixture was heated to 90° C. and aged for 1 hour. The mixture was then allowed to stand at room temperature for a further 16 hours. The resulting brown precipitate was washed by centrifugation, oven dried at 120° C. for 16 hours and milled. The product yield was 140 g.
  • a suspension of 44.80 g of a silica gel having an average particle size of about 3 ⁇ m in 362.00 g of demineralised water was prepared. Under constant stirring, 44.20 g of calcium hydroxide (0.60 moles) was added and the pH allowed to stabilise. 62.11 g of a 50% solution of HPA (0.20 moles) was then added under stirring over a period of about 15 minutes at a rate of 3 ml/minute. During the addition, the temperature reached about 40-50° C. The reaction mixture was heated to 90° C. and aged for 1 hour. The mixture was then allowed to stand at room temperature for a further 16 hours. Thereupon, the brown precipitate was washed by centrifugation, oven dried at 120° C. for 16 hours and milled. The product yield was 103 g.
  • a suspension of 44.80 g of a silica gel having an average particle size of about 3 ⁇ m in 362.00 g of demineralised water was prepared. Under constant stirring, 44.20 g of calcium hydroxide (0.60 moles) was added and the pH allowed to stabilise. 62.11 g of a 50% solution of HPA (0.20 moles) was then added under stirring over a period of about 15 minutes at a rate of 3 ml/minute. During the addition, the temperature reached about 40-50° C. After the pH had stabilised, a further 48.40 g of zinc oxide (0.60 moles) was stirred in. The reaction mixture was heated to 90° C. and aged for 1 hour. The mixture was then allowed to stand at room temperature for a further 16 hours. The resulting brown precipitate was washed by centrifugation, oven dried at 120° C. for 16 hours and milled. The product yield was 149 g.
  • a suspension of 44.80 g of a silica gel having an average particle size of about 3 ⁇ m in 362.00 g of demineralised water was prepared. Under constant stirring, 72.90 g of zinc oxide (0.90 moles) was added and the pH allowed to stabilise. 93.60 g of a 50% solution of HPA (0.30 moles) was then added under stirring over a period of about 30 minutes at a rate of 3 ml/minute. During the addition, the temperature reached about 40-50° C. After the pH had stabilised, a further 24.30 g of zinc oxide (0.30 moles) was stirred in. The reaction mixture was heated to 90° C. and aged for 1 hour. The mixture was then allowed to stand at room temperature for a further 16 hours. The resulting brown precipitate was washed by centrifugation, oven dried at 120° C. for 16 hours and milled. The product yield was 159 g.
  • a suspension of 44.80 g of a silica gel having an average particle size of about 3 ⁇ m in 244.45 g of demineralised water was prepared. Under constant stirring, 42.18 g of calcium hydroxide (0.57 moles) was added followed by 18.95 g of zinc oxide (0.23 moles) and the pH allowed to stabilise. 123.55 g of a 50% solution of HPA (0.40 moles) was then added under stirring over a period of about 35 minutes at a rate of 3 ml/minute. During the addition, the temperature reached about 40-50° C. After the pH had stabilised, a further 24.30 g of zinc oxide (0.30 moles) was stirred in. The reaction mixture was heated to 90° C. and aged for 1 hour. The mixture was then allowed to stand at room temperature for a further 16 hours. The resulting brown precipitate was washed by centrifugation, oven dried at 120° C. for 16 hours and milled. The product yield was 169 g.
  • a suspension of 45.00 g of a silica gel having an average particle size of about 3 ⁇ m in 386.70 g of demineralised water was prepared. Under constant stirring, 42.18 g of calcium hydroxide (0.57 moles) was added and the pH allowed to stabilise. 58.80 g of a 50% solution of HPA (0.19 moles) was then added under stirring at a rate of 3 ml/minute. After the pH had stabilised, 9.43 g of magnesium oxide (0.23 moles) was stirred in and a further 44.66 g of 50% HPA solution (0.16 moles) was added at a rate of 3 ml/minute. During the addition, the temperature reached about 40-50° C.
  • a suspension of 44.80 g of a silica gel having an average particle size of about 3 ⁇ m in 362.00 g of demineralised water was prepared. Under constant stirring, 44.20 g of calcium hydroxide (0.60 moles) was added and the pH allowed to stabilise. 59.51 g of a 50% solution of ATMP (0.10 moles) was then added under stirring over a period of about 15 minutes at a rate of 3 ml/minute. During the addition, the temperature reached about 40° C. The reaction mixture was heated to 90° C. and aged for 1 hour. The mixture was then allowed to stand at room temperature for a further 16 hours. The resulting white precipitate was washed by centrifugation, oven dried at 120° C. for 16 hours and milled. The product yield was 106 g.
  • a suspension of 20.63 g of silica gel having an average particle size of about 3 ⁇ m in 80.36 g demineralised water was prepared. 11.84 g of zinc chloride (0.087 moles) and 13.15 g of calcium chloride dihydrate (0.089 moles) were dissolved in the suspension. 19.28 g of a 50% solution of HPA (0.062 moles) was then added, and the pH was increased to 6 by the addition of 2M NaOH at a rate of 3 ml/min. The reaction mixture was aged for 24 hours at room temperature. The resulting brown precipitate was filtered, washed, oven dried at 120° C. for 16 hours and milled. The product yield was 25 g.
  • Zinc potassium chromate, strontium chromate, zinc phosphate (SICOR ZNP/M and HEUCOPHOS ZMP), aluminium triphosphate-based pigments (K-White 84, 105, 140W), and calcium-exchanged silica (SHIELDEX AC5) pigments were used to judge the performance of the pigments of the present invention.
  • the above mentioned pigments of sections A and B were evaluated in various anti-corrosive coating systems as given below.
  • the paints were applied to test panels by bar coater to specified film thicknesses and allowed to dry or cure according to the requirements of the paint system.
  • the panels were then scribed and tested in salt spray (ASTM B117), humidity (DIN 50017) or immersed in water for varying periods of time. After testing, the panels were examined immediately for blistering, scribe rusting, scribe adhesion loss, adhesion loss over the panel and through-film corrosion.
  • salt spray ASTM B117
  • humidity DIN 50017
  • the panels were examined immediately for blistering, scribe rusting, scribe adhesion loss, adhesion loss over the panel and through-film corrosion.
  • the following standards were employed:
  • Pigments taken from groups A and B were tested in various water-borne and non-aqueous solvent-borne resin systems. Resins used for this purpose and conditions of test are given below.
  • Items 1-9 below were dispersed to 25 ⁇ m using a pearl mill. Items 10 and 11 were added with stirring. Items 12-14 were premixed and added after ageing the paint overnight to achieve a paint having a pigment volume concentration (PVC) of 25% and 54 wt. % solids.
  • PVC pigment volume concentration
  • Comparison examples A1 and A2 were also prepared using the above formulation. Additional comparison examples were prepared as follows with the amount of talc being adjusted to maintain PVC at 25%.
  • Modified Aluminium Triphosphate 7.5 wt. % K-White 105.
  • Paints were applied to degreased cold rolled steel test panels (Q-Panels S412) to a dry film thickness of about 80 ⁇ m.
  • the coated panels were allowed to dry for 7 days at room temperature before testing under salt spray and water soak conditions for a period of 240 hours. Test results are given in Table 1.
  • Comparison examples A1 and A2 were also prepared using the above formulation. Additional comparison examples were prepared as follows with the amount of talc being adjusted to maintain PVC at 25%.
  • Modified Aluminium Triphosphate 7.8 wt. % K-White 105.
  • Paints were applied to degreased cold rolled steel test panels (Q-Panels S412) to a dry film thickness of about 40 ⁇ m.
  • the coated panels were allowed to dry for 7 days at room temperature before testing under salt spray and water soak conditions for a period of 240 hours. Test results are given in Table 2.
  • Comparison examples were prepared as follows with the amount of talc being adjusted to maintain PVC at 25%. All formulations contained about 1 wt. % ZnO.
  • Paints were applied to degreased cold rolled steel test panels (Q-Panels S412) to a dry film thickness of about 40 ⁇ m.
  • the coated panels were allowed to dry for 7 days at room temperature before testing under salt spray and water soak conditions for a period of 240 hours.
  • 1% ZnO was included in all the formulations tested. Test results are given in Table 3.
  • Comparison examples were prepared as follows with the amount of talc and Plastorit being adjusted to maintain PVC at 30%.
  • Paints were applied to degreased cold rolled steel test panels (Q-Panels S412) to a dry film thickness of about 40 ⁇ m.
  • the coated panels were allowed to dry for 7 days at room temperature before testing under salt spray and water soak conditions for a period of 240 hours. Test results are given in Table 4.
  • Comparison examples were prepared as follows with the amount of talc and Plastorit being adjusted to maintain PVC at 30%.
  • Paints were applied to degreased cold rolled steel test panels (Q-Panels S412) to a dry film thickness of about 40 ⁇ m.
  • the coated panels were allowed to dry for 7 days at room temperature before testing under salt spray and water soak conditions for a period of 240 hours. Test results are given in Table 5.
  • Comparison examples were prepared as follows with the amount of Tiona 472 being adjusted to maintain PVC at 20%.
  • Comparison examples were prepared as follows with the amount of Tiona 472 being adjusted to maintain PVC at 20%.
  • Items 1-9 were dispersed in a pearl mill. Items 10-13 were mixed separately and added to items 1-9. Items 14-18 were mixed separately and added to items 1-13.

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  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
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  • Pigments, Carbon Blacks, Or Wood Stains (AREA)
  • Sealing Material Composition (AREA)
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US09/029,478 1995-08-25 1996-08-15 Anti-corrosive pigment and compositions formulated with such pigments Expired - Lifetime US6083308A (en)

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Cited By (13)

* Cited by examiner, † Cited by third party
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US6447594B1 (en) 2001-06-13 2002-09-10 Wayne Pigment Corporation Strontium chromate corrosion inhibitor pigment with reduced solubility
US20030216049A1 (en) * 2000-12-01 2003-11-20 Applied Materials, Inc. Method and composition for the removal of residual materials during substrate planarization
WO2004033115A1 (en) * 2002-10-04 2004-04-22 Northern Illinois University In situ phosphatizing and silicating coatings and method of making same
US20050065269A1 (en) * 2002-01-24 2005-03-24 Horst Hintze-Bruning Anti-corrosive mixture and coating substances containing said anti-corrosive mixture
US20050085565A1 (en) * 2002-01-24 2005-04-21 Horst Hintze-Bruning Coating materials and the use thereof for producing coatings which can be soldered
US20060214137A1 (en) * 2005-03-25 2006-09-28 Bulk Chemicals, Inc. Phosphonic acid and polyvinyl alcohol conversion coating
US20070012220A1 (en) * 2004-03-18 2007-01-18 Dai Nippon Toryo Co., Ltd. Environmentally Pollution-Free Anti-Corrosion Pigment Composition
US20070141369A1 (en) * 2005-12-19 2007-06-21 General Electric Company Strain tolerant corrosion protecting coating and spray method of application
US20080054806A1 (en) * 2005-05-10 2008-03-06 Alvarez Khristopher E Process for Minimizing Electromigration in an Electronic Device
US20110233473A1 (en) * 2008-12-08 2011-09-29 Grace Gmbh & Co. Kg Anti-corrosive particles
US8791191B2 (en) 2009-02-03 2014-07-29 Buehler Partec Gmbh Zinc oxide particles which have been modified with phosphonocarboxylic acid and use of zinc oxide particles
US20140272133A1 (en) * 2013-03-15 2014-09-18 Ecolab Usa Inc. Corrosion control compositions and methods of mitigating corrosion
US10385216B2 (en) 2007-11-19 2019-08-20 Grace Gmbh Anti-corrosive particles

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AU759529B2 (en) * 1999-03-12 2003-04-17 Akzo Nobel N.V. Filler composition
EP2241602A1 (de) 2009-04-17 2010-10-20 Bühler PARTEC GmbH Mit Phosphonocarbonsäure modifizierte Zinkoxid-Partikel und Verwendung von Zinkoxid-Partikeln
RU2505571C1 (ru) * 2012-07-20 2014-01-27 Общество с ограниченной ответственностью "Научно-производственное предприятие "ПигБи" (ООО "НПП "ПигБи") Способ получения противокоррозионного пигмента
US10131813B2 (en) 2015-07-22 2018-11-20 Dow Global Technologies Llc Ambient cure compositions for making coatings having humidity and corrosion resistance and methods of use
US10669429B2 (en) 2015-07-22 2020-06-02 Dow Global Technologies Llc Ambient cure compositions for making coatings having humidity and corrosion resistance and methods of use

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EP0096526A2 (de) * 1982-06-01 1983-12-21 INTERNATIONAL PAINT Public Limited Company Rostschützende Farbe
JPS60256377A (ja) * 1984-04-16 1985-12-18 ナ−ムロ−ズ・ベンノットシヤップ・イノゲネ−テイクス 食細胞セルラインの分析への利用
EP0389653A1 (de) * 1989-03-29 1990-10-03 Tayca Corporation Antikorrosive Pigmentzusammensetzung und diese enthaltende antikorrosive Überzugsmasse
EP0634460A2 (de) * 1993-07-13 1995-01-18 ALBRIGHT & WILSON UK LIMITED Antikorrosive Pigmente

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JPS60124660A (ja) * 1983-12-12 1985-07-03 Nippon Chem Ind Co Ltd:The 防錆顔料

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Publication number Priority date Publication date Assignee Title
EP0096526A2 (de) * 1982-06-01 1983-12-21 INTERNATIONAL PAINT Public Limited Company Rostschützende Farbe
JPS60256377A (ja) * 1984-04-16 1985-12-18 ナ−ムロ−ズ・ベンノットシヤップ・イノゲネ−テイクス 食細胞セルラインの分析への利用
EP0389653A1 (de) * 1989-03-29 1990-10-03 Tayca Corporation Antikorrosive Pigmentzusammensetzung und diese enthaltende antikorrosive Überzugsmasse
EP0634460A2 (de) * 1993-07-13 1995-01-18 ALBRIGHT & WILSON UK LIMITED Antikorrosive Pigmente

Cited By (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030216049A1 (en) * 2000-12-01 2003-11-20 Applied Materials, Inc. Method and composition for the removal of residual materials during substrate planarization
US6447594B1 (en) 2001-06-13 2002-09-10 Wayne Pigment Corporation Strontium chromate corrosion inhibitor pigment with reduced solubility
US7202294B2 (en) 2002-01-24 2007-04-10 Basf Coatings Ag Coating materials and the use thereof for producing coatings which can be soldered
US20050065269A1 (en) * 2002-01-24 2005-03-24 Horst Hintze-Bruning Anti-corrosive mixture and coating substances containing said anti-corrosive mixture
US20050085565A1 (en) * 2002-01-24 2005-04-21 Horst Hintze-Bruning Coating materials and the use thereof for producing coatings which can be soldered
US7220298B2 (en) 2002-01-24 2007-05-22 Basf Coatings Ag Anti-corrosive mixture and coating substances containing said anti-corrosive mixture
WO2004033115A1 (en) * 2002-10-04 2004-04-22 Northern Illinois University In situ phosphatizing and silicating coatings and method of making same
US20070012220A1 (en) * 2004-03-18 2007-01-18 Dai Nippon Toryo Co., Ltd. Environmentally Pollution-Free Anti-Corrosion Pigment Composition
US20090078158A1 (en) * 2004-03-18 2009-03-26 Dai Nippon Toryo Co., Ltd. Environmentally pollution-free anti-corrosion pigment composition
CN1934204B (zh) * 2004-03-18 2010-08-18 大日本涂料株式会社 无公害防锈颜料组合物
US7828884B2 (en) 2004-03-18 2010-11-09 Dai Nippon Toryo Co., Ltd. Environmentally pollution-free anti-corrosion pigment composition
US7935274B2 (en) * 2005-03-25 2011-05-03 Bulk Chemicals, Inc. Phosphonic acid and polyvinyl alcohol conversion coating
US20060214137A1 (en) * 2005-03-25 2006-09-28 Bulk Chemicals, Inc. Phosphonic acid and polyvinyl alcohol conversion coating
US8450931B2 (en) 2005-05-10 2013-05-28 Dow Corning Corporation Process for minimizing electromigration in an electronic device
US20080054806A1 (en) * 2005-05-10 2008-03-06 Alvarez Khristopher E Process for Minimizing Electromigration in an Electronic Device
US7754342B2 (en) 2005-12-19 2010-07-13 General Electric Company Strain tolerant corrosion protecting coating and spray method of application
US20070141369A1 (en) * 2005-12-19 2007-06-21 General Electric Company Strain tolerant corrosion protecting coating and spray method of application
US10385216B2 (en) 2007-11-19 2019-08-20 Grace Gmbh Anti-corrosive particles
US20110233473A1 (en) * 2008-12-08 2011-09-29 Grace Gmbh & Co. Kg Anti-corrosive particles
US9403994B2 (en) * 2008-12-08 2016-08-02 Grace Gmbh & Co. Kg Anti-corrosive particles
US8791191B2 (en) 2009-02-03 2014-07-29 Buehler Partec Gmbh Zinc oxide particles which have been modified with phosphonocarboxylic acid and use of zinc oxide particles
US20140272133A1 (en) * 2013-03-15 2014-09-18 Ecolab Usa Inc. Corrosion control compositions and methods of mitigating corrosion
US9175405B2 (en) * 2013-03-15 2015-11-03 Ecolab Usa Inc. Corrosion control compositions and methods of mitigating corrosion
US10443133B2 (en) 2013-03-15 2019-10-15 Ecolab Usa Inc. Corrosion control compositions and methods of mitigating corrosion
US11155927B2 (en) 2013-03-15 2021-10-26 Ecolab Usa Inc. Corrosion control compositions and methods of mitigating corrosion

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DE69533671D1 (de) 2004-11-25
BR9610024A (pt) 1999-07-06
DE69533671T8 (de) 2006-06-08
DE69533671T2 (de) 2006-03-09
KR19990044121A (ko) 1999-06-25
JPH11512126A (ja) 1999-10-19
ATE280202T1 (de) 2004-11-15
AU6924696A (en) 1997-03-19
EP0760387B1 (de) 2004-10-20
ES2231777T3 (es) 2005-05-16
KR100499215B1 (ko) 2005-09-09
WO1997008245A1 (en) 1997-03-06
DK0760387T3 (da) 2005-01-10
EP0760387A1 (de) 1997-03-05
JP4082726B2 (ja) 2008-04-30

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